"Ambry Genetics"[submitter] AND "SFRP4"[gene] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2365999	NM_003014.4(SFRP4):c.1024A>T (p.Asn342Tyr)	SFRP4 (N342Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2535418	NM_003014.4(SFRP4):c.1001C>T (p.Thr334Ile)	SFRP4 (T334I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1377522	NM_003014.4(SFRP4):c.947C>A (p.Pro316Gln)	SFRP4 (P316Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2307202	NM_003014.4(SFRP4):c.938C>T (p.Pro313Leu)	SFRP4 (P313L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2204343	NM_003014.4(SFRP4):c.916G>A (p.Gly306Arg)	SFRP4 (G306R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2249684	NM_003014.4(SFRP4):c.911C>G (p.Thr304Arg)	SFRP4 (T304R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2522098	NM_003014.4(SFRP4):c.706C>T (p.Pro236Ser)	SFRP4 (P236S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2319741	NM_003014.4(SFRP4):c.608T>G (p.Ile203Arg)	SFRP4 (I203R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2309814	NM_003014.4(SFRP4):c.575G>T (p.Ser192Ile)	SFRP4 (S192I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2544053	NM_003014.4(SFRP4):c.561G>C (p.Leu187Phe)	SFRP4 (L187F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2483514	NM_003014.4(SFRP4):c.444G>T (p.Glu148Asp)	SFRP4 (E148D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2252187	NM_003014.4(SFRP4):c.377A>G (p.Asp126Gly)	SFRP4 (D126G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1428250	NM_003014.4(SFRP4):c.310G>A (p.Ala104Thr)	SFRP4 (A104T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1439109	NM_003014.4(SFRP4):c.214G>T (p.Val72Leu)	SFRP4 (V72L)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2214371	NM_003014.4(SFRP4):c.106C>A (p.Pro36Thr)	SFRP4 (P36T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1477334	NM_003014.4(SFRP4):c.37C>A (p.Leu13Met)	SFRP4 (L13M)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2547480	NM_003014.4(SFRP4):c.35G>C (p.Trp12Ser)	SFRP4 (W12S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance